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NCT02227797 · ClinicalTrials.gov registry record · Phase 1
MT2013-37R: Voriconazole Monitoring in Pediatric Stem Cell Transplant Patients
A Phase 1 study, sponsored by Masonic Cancer Center, University of Minnesota.
- Completed
- Registry status
- Phase 1
- Development phase
- 66
- Enrollment target
NCT02227797: Completed Phase 1 study, sponsored by Masonic Cancer Center, University of Minnesota.
NCT02227797 is a Phase 1 study that has completed, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 66 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02227797, a Phase 1 study, has completed, sponsored by Masonic Cancer Center, University of Minnesota.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 66 participants
- Enrollment target
Study Summary
The primary purpose of this study is to identify the optimal dose of voriconazole, an anti-fungal drug often used in people undergoing stem cell transplant. An optimal dose level is one level that provides a good blood level (concentration) of voriconazole without too much toxicity.
Interventions
- DRUG Voriconazole
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2015-01-19 |
| Est. Completion | 2019-03-01 |
| Phase | Phase 1 |
What the finished NCT02227797 record still lists
NCT02227797 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 66 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (10% higher).
The record links to 0 conditions, and to 1 intervention - of which Voriconazole is the first listed.
NCT02227797 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02227797 about?
NCT02227797 is a clinical study titled "MT2013-37R: Voriconazole Monitoring in Pediatric Stem Cell Transplant Patients". The primary purpose of this study is to identify the optimal dose of voriconazole, an anti-fungal drug often used in people undergoing stem cell transplant. An optimal dose level is one level that provides a good blood level (concentration) of voriconazole without too much toxicity.
What is the current status of trial NCT02227797?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 66 participants. The study started on 2015-01-19. Estimated completion is 2019-03-01.
What interventions are being tested in trial NCT02227797?
The interventions under investigation include: Voriconazole (DRUG).
Who is sponsoring clinical trial NCT02227797?
This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02227797's enrollment target sits among peer trials
66 786th of 2000 higher than 1,203 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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